Allele Registry

Canonical Allele Identifier: PA645378990

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000232347

RCV000561246

RCV000582421

RCV003233509

RCV003463644

RCV003491994

RCV003998733

ClinVar Variation:

237215

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly273Val	CA073459 NM_000179.3:c.818G>T